chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56484922964849230AC16GENIChomozygous113835777
56485031564850316GA15GENIChomozygous114207773
56485091364850914AT19GENIChomozygous114207774
56485484064854840AT21GENIChomozygous132626091
56485528464855285CG18GENIChomozygous113835781
56485585164855852AG20GENIChomozygous113835783
56485649164856492AG22GENIChomozygous113835784
56485756564857566GA13GENIChomozygous113835785
56485777764857778AG20GENIChomozygous113835786
56485803064858031GA19GENIChomozygous114207776
56485822364858224TA22GENIChomozygous113835788
56485933164859332AC30GENIChomozygous114207779
56485993764859938GA18GENIChomozygous114207780
56486010664860107GA22GENIChomozygous113835789
56486025764860258CT17GENIChomozygous114207781
56486096164860962GA25GENIChomozygous113835793
56486105864861059TC25GENIChomozygous113835795
56486122864861229AG17GENIChomozygous113835796
56486174464861745GA19GENIChomozygous114207783
56485748764857488CA6GENIChomozygous114119624
56486183264861833GT22GENIChomozygous114207784
56486248064862481TG16GENIChomozygous114207785
56486277064862771CT19GENIChomozygous114207786
56485724664857247GA10GENIChomozygous128287924
56485724864857249AT11GENIChomozygous128287925
56485838464858384A15GENIChomozygous128192274
56485866764858668T29GENICpossibly homozygous128192275
56486253864862538T13GENIChomozygous128192276
56486427464864275G17GENIChomozygous128192278
56486447364864474TG22GENIChomozygous113835803
56486449664864497AT22GENIChomozygous113835804
56486449764864498AC22GENIChomozygous113835805
56486428064864281GA18GENIChomozygous118843159